drugset / Trial / NCT00142116

Summary

The purpose of this study is to determine the percentage of people who can attain remission and the length of time such responses to therapy are sustained, as well as the side effects that might result from rituximab and thalidomide in people with lymphoplasmacytic lymphoma.

Timeline

Start
2003-05
Primary completion
2004-02
Completion
2008-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous
Subject Thalidomide Other / unclassified 400 mg Oral